2020
Repurposing Tyrosine Kinase Inhibitors to Overcome Multidrug Resistance in Cancer: A Focus on Transporters and Lysosomal Sequestration
KRCHNIAKOVÁ, Mária, Jan ŠKODA, Jakub NERADIL, Petr CHLAPEK, Renata VESELSKÁ et. al.Základní údaje
Originální název
Repurposing Tyrosine Kinase Inhibitors to Overcome Multidrug Resistance in Cancer: A Focus on Transporters and Lysosomal Sequestration
Autoři
KRCHNIAKOVÁ, Mária (703 Slovensko, domácí), Jan ŠKODA (203 Česká republika, domácí), Jakub NERADIL (203 Česká republika, domácí), Petr CHLAPEK (203 Česká republika, domácí) a Renata VESELSKÁ (203 Česká republika, garant, domácí)
Vydání
International Journal of Molecular Sciences, Basel, MDPI, 2020, 1422-0067
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10608 Biochemistry and molecular biology
Stát vydavatele
Švýcarsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 5.923
Kód RIV
RIV/00216224:14310/20:00118624
Organizační jednotka
Přírodovědecká fakulta
UT WoS
000535581700128
Klíčová slova anglicky
tyrosine kinase inhibitor; multidrug resistance; cancer; ABC transporter; SLC transporter; lysosomal sequestration
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 31. 8. 2021 16:29, Mgr. Marie Šípková, DiS.
Anotace
V originále
Tyrosine kinase inhibitors (TKIs) are being increasingly used to treat various malignancies. Although they were designed to target aberrant tyrosine kinases, they are also intimately linked with the mechanisms of multidrug resistance (MDR) in cancer cells. MDR-related solute carrier (SLC) and ATB-binding cassette (ABC) transporters are responsible for TKI uptake and efflux, respectively. However, the role of TKIs appears to be dual because they can act as substrates and/or inhibitors of these transporters. In addition, several TKIs have been identified to be sequestered into lysosomes either due to their physiochemical properties or via ABC transporters expressed on the lysosomal membrane. Since the development of MDR represents a great concern in anticancer treatment, it is important to elucidate the interactions of TKIs with MDR-related transporters as well as to improve the properties that would prevent TKIs from diffusing into lysosomes. These findings not only help to avoid MDR, but also help to define the possible impact of combining TKIs with other anticancer drugs, leading to more efficient therapy and fewer adverse effects in patients.
Návaznosti
NV17-33104A, projekt VaV |
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